Cytogenetic analysis of a pediatric T-cell acute lymphoblastic leukemia (ALL) cell line (HPB-ALL) revealed the cryptic t(5;14)(q35;q32.2), recently found in 15-20% pediatric T-ALL patients, with 5q35 and 14q32.2 breakpoints at 5'-HOX11L2 and 3'-BCL11B, respectively. Expression of both BCL11B, which
14q32/miRNA Clusters loss of heterozygosity in acute lymphoblastic leukemia is associated with up-regulation of BCL11a
✍ Scribed by Cecilia Agueli; Giuseppe Cammarata; Domenico Salemi; Lea Dagnino; Roberta Nicoletti; Maria La Rosa; Francesca Messana; Anna Marfia; Maria Grazia Bica; Maria Luisa Coniglio; Maria Pagano; Francesco Fabbiano; Alessandra Santoro
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 217 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0361-8609
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✦ Synopsis
Abstract
This study evaluated the loss and expression level of miRNAs 14q32 clusters in acute lymphoblastic leukemia (ALL) patients with cryptic deletions at 14q32 chromosomal band to investigate their involvement in this disease. We demonstrate that a subset of ALL cases bearing 14q32 LOH showed a down‐regulation of miRNA 14q32 clusters, which is directly linked to the submicroscopic chromosomal deletion. As a consequence of miRNAs deregulation we reported an inverse correlation with the expression of their target BCL11a, a transcription factor involved in lymphoid differentiation. These results suggest that 14q32/miRNA clusters LOH may be another mechanism involved in lymphoid B cell transformation and differentiation and therefore, could be used as a diagnostic marker and therapeutic target in subsets of ALL. Am. J. Hematol., 2010. © 2010 Wiley‐Liss, Inc.
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